In silico analysis of single nucleotide polymorphisms (SNPs) in human FOXC2 gene

Introduction: Lymphedema is an abnormal accumulation of interstitial fluid, due to inefficient uptake and reduced flow, leading to swelling and disability, mostly in the extremities. Hereditary lymphedema usually occurs as an autosomal dominant trait with allelic heterogeneity. Methods: We identifie...

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Dades bibliogràfiques
Publicat a:F1000Res
Autors principals: Nimir, Mohammed, Abdelrahim, Mohanad, Abdelrahim, Mohamed, Abdalla, Mahil, Ahmed, Wala eldin, Abdullah, Muhanned, Hamid, Muzamil Mahdi Abdel
Format: Artigo
Idioma:Inglês
Publicat: F1000 Research Limited 2017
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5814747/
https://ncbi.nlm.nih.gov/pubmed/29511529
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.10937.2
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